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胫骨先天性间叶瘤:病例报告及文献复习。

Congenital mesenchymoma of tibia: case report and review of literature.

机构信息

Department of Orthopedics, Post Graduate Institute of Medical Education and Research, Chandigarh 160012, India.

出版信息

J Pediatr Surg. 2012 Dec;47(12):e17-20. doi: 10.1016/j.jpedsurg.2012.08.039.

Abstract

Fibrocartilaginous mesenchymoma is a rare bone tumor arising from long bones in children and adolescents. With only 21 cases reported in the literature, it is often not included in the differential diagnosis in patients with a bone tumor. Previously, the youngest case reported was in a 19-month-old boy, and a congenital variant had not been reported. We describe a case of congenital fibrocartilaginous mesenchymoma of the proximal tibia that presented shortly after birth. Biopsy of a suspected malignancy on imaging confirmed the diagnosis. The child was temporarily lost to follow up and presented again with genu varum and limb shortening but surprisingly, the tumor had completely resolved without surgical intervention.

摘要

纤维软骨性间叶瘤是一种罕见的骨肿瘤,发生于儿童和青少年的长骨。文献中仅报道了 21 例,因此在骨肿瘤患者的鉴别诊断中通常不包括这种肿瘤。此前,报告的最小年龄为 19 个月大的男孩,且尚未报道先天性变异。我们描述了一例出生后不久即出现的胫骨近端先天性纤维软骨性间叶瘤。影像学检查怀疑为恶性肿瘤而进行的活检证实了该诊断。患儿暂时失访,再次就诊时出现膝内翻和肢体缩短,但令人惊讶的是,肿瘤未经手术干预完全消退。

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